IntelliVue Patient Monitor MX700Recalls & reported problems

Summary

The FDA's MAUDE database contains 76 adverse event reports that list this exact device (DI 00884838029088), received between May 14, 2018 and Sep 22, 2026 — classified as 6 deaths, 10 injuries, 60 malfunctions.

The most frequently reported specific device problem is “No Audible Alarm” (27 reports).

1 FDA recall record name this device's identifier, 1 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Recalls naming this device

1. Oct 31, 2025Class IIOpen, Classified

   Potential issue where the IntelliVue monitors did not alarm.

   Z-0867-2026 · Root cause: Use error · Recall details · FDA record ↗

Most reported problems

Recent adverse event reports

The 25 most recent of 76 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 22, 2026Incorrect Measurement

  Philips received a complaint on an IntelliVue MX700 patient monitor indicating a discrepancy in SPO2 readings. The device was not in clinical use at time of event; there was no adverse event reported.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50858784 ↗
• MalfunctionMay 12, 2026Defective Alarm

  IT WAS REPORTED THAT MONITOR DID NOT GENERATE AN ALARM FOR A HIGH HEART RATE. THE DEVICE WAS IN USE ON A PATIENT AT THE TIME OF THE EVENT. THERE WAS NO ADVERSE EVENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25148493 ↗
• MalfunctionMay 7, 2026Defective Alarm

  IT WAS REPORTED THAT THAT THE ARTERIAL BLOOD PRESSURE (ABP) ALARMS ARE NOT FUNCTIONING PROPERLY. THE DEVICE WAS IN USE ON A PATIENT AT THE TIME OF THE EVENT. THERE WAS NO ADVERSE EVENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25111884 ↗
• MalfunctionMar 17, 2026Device Fell

  IT WAS REPORTED THAT A X2 MEASUREMENT SERVER FELL OF THE MOUNT. THE DEVICE WAS IN CLINICAL USE. THERE WAS NO REPORT OF PATIENT OR USER HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24615997 ↗
• MalfunctionMar 9, 2026No Audible Alarm

  PHILIPS RECEIVED A COMPLAINT ON THE INTELLIVUE MX700 PATIENT MONITOR INDICATING THAT THERE WAS A SPEAKER FAILURE. THE DEVICE WAS NOT IN USE ON PATIENT AT TIME OF EVENT, THERE WAS NO ADVERSE EVENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24551655 ↗
• MalfunctionMar 6, 2026Defective Alarm

  IT WAS REPORTED THE CUSTOMER MISSED A YELLOW NON-INVASIVE BLOOD PRESSURE ALARM. THERE WAS NO REPORT OF ACTUAL HARM ASSOCIATED WITH THIS COMPLAINT. THE CUSTOMER REQUESTED ASSISTANCE DETERMINING WHY THE YELLOW NIBP ALARM WAS NOT DISPLAYED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24533297 ↗
• MalfunctionJan 21, 2026Defective Alarm

  IT WAS REPORTED THAT THE DEVICE DID NOT GENERATE AN ALARM FOR DESATURATION. THE DEVICE WAS IN USE ON A PATIENT. THERE WAS NO REPORT OF PATIENT OR USER HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24128077 ↗
• MalfunctionJan 3, 2026No Audible Alarm

  IT WAS REPORTED THERE IS NO ALARM WHEN THE LOWER LIMIT OF PULSE OXYGEN IS REACHED. THE DEVICE WAS IN USE ON A PATIENT AT THE TIME OF THE EVENT, THERE WAS NO ADVERSE EVENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23953580 ↗
• MalfunctionDec 9, 2025Defective Alarm; Defective Alarm

  IT WAS REPORTED THE CUSTOMER MISSED A YELLOW NON-INVASIVE BLOOD PRESSURE ALARM. THERE WAS NO REPORT OF ACTUAL HARM ASSOCIATED WITH THIS COMPLAINT. THE CUSTOMER REQUESTED ASSISTANCE DETERMINING WHY THE YELLOW NIBP ALARM WAS NOT DISPLAYED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23758479 ↗
• InjuryNov 13, 2025Defective Alarm; Defective Alarm

  IT WAS REPORTED THE NURSES DID NOT HEAR AN ALARM GENERATED FOR A DESATURATION EVENT. THE STAFF DISCOVERED THE PATIENT, AN INFANT, THAT WAS BLUE IN COLOR AND INITIATED RESUSCITATION. IT WAS NOTED THERE WAS NO ALARM PRIOR TO THE PATIENT BEING FOUND BUT THAT AN ALARM WAS GENERATED AFTER RESUSCITATION BEGAN.

  Patient problems: Insufficient Information

  MAUDE report 23547035 ↗
• MalfunctionJul 8, 2025No Audible Prompt/Feedback; No Audible Prompt/Feedback

  IT WAS REPORTED THE SPEAKER IS NOT WORKING. IT IS UNKNOWN AT THIS TIME IF THERE WAS SOUND. IT IS UNKNOWN IF THE DEVICE WAS IN CLINICAL USE AT THE TIME OF THE EVENT. NO ADVERSE EVENT OR PATIENT HARM WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22435003 ↗
• InjuryJun 25, 2025Excessive Heating; Excessive Heating

  IT WAS REPORTED THE PATIENT DEVELOPED A BURN AT THE ELECTRODE SITE WHILE BEING MONITORED. AN UNKNOWN MEDICAL INTERVENTION OCCURRED, AND THE BURN WAS EXPECTED TO HEAL COMPLETELY WITH NO PERMANENT DAMAGE. THE BURN DID NOT OCCUR DURING AN MRI. NO OTHER CLINICAL INFORMATION WAS PROVIDED; THEREFORE, GOOD FAITH EFFORTS ARE BEING PERFORMED.

  Patient problems: Insufficient Information

  MAUDE report 22326299 ↗
• InjuryApr 23, 2025Defective Alarm; Defective Alarm

  IT WAS REPORTED THAT THERE WAS AN ALARM PROBLEM. NO OTHER CLINICAL INFORMATION OR MEDICAL INTERVENTION WAS REPORTED; THEREFORE, GOOD FAITH EFFORTS ARE BEING PERFORMED.

  Patient problems: Tachycardia

  MAUDE report 21894423 ↗
• MalfunctionApr 23, 2025Defective Alarm; Defective Alarm

  PHILIPS RECEIVED A COMPLAINT ON THE INTELLIVUE MX700 PATIENT MONITOR INDICATING THAT THE MACHINE DID NOT ALARM WHEN THE PATIENT WAS DE-SATING. THE DEVICE WAS IN USE ON A PATIENT AT THE TIME OF THE EVENT. THERE WAS NO ADVERSE EVENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21890112 ↗
• MalfunctionMar 25, 2025No Audible Prompt/Feedback; No Audible Prompt/Feedback

  PHILIPS RECEIVED A COMPLAINT ON AN INTELLIVUE MX700 PATIENT MONITOR INDICATING THAT THERE WAS A "SPEAKER MALFUNCTION" ERROR WHILE USING A BEDSIDE MONITOR AND AN X3 ON A PATIENT. THE CUSTOMER BIOMEDICAL ENGINEER (BIOMED) WANTED TO DETERMINE WHETHER THE ISSUE ORIGINATED FROM THE MX700 BEDSIDE MONITOR OR THE X3. IT WAS NOT KNOWN IF THE SPEAKER WAS ABLE TO PRODUCE SOUND. THE DEVICE WAS IN CLINICAL USE AT THE TIME THE ISSUE WAS DISCOVERED. THERE WAS NO ADVERSE EVENT OR PATIENT HARM REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21686654 ↗
• MalfunctionDec 5, 2024No Audible Alarm; No Audible Alarm

  PHILIPS RECEIVED A COMPLAINT ON THE INTELLIVUE MX700 PATIENT MONITOR INDICATING THAT THE PAUSE ALARM DID NOT RING EVEN THOUGH THE CLINICAL AUDIT INDICATES THE PRESENCE OF PAUSE AND ASYSTLY ALARMS. THE DEVICE WAS IN USE ON A PATIENT AT TIME OF EVENT, THERE WAS NO ADVERSE EVENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20855187 ↗
• MalfunctionJun 24, 2024No Audible Alarm; No Audible Prompt/Feedback; No Audible Alarm; No Audible Prompt/Feedback

  IT WAS REPORTED THAT THE TONE DOES NOT SOUND WITH POWER LOSS ON THE DEVICE. THE DEVICE WAS NOT IN USE ON PATIENT AT TIME OF EVENT, THERE WAS NO ADVERSE EVENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19597609 ↗
• MalfunctionJun 11, 2024Defective Alarm; Defective Alarm

  PHILIPS RECEIVED A COMPLAINT ON THE INTELLIVUE MX700 PATIENT MONITOR INDICATING THAT THE ART ALARM WAS RINGING AS A YELLOW ALARM WHEN IT SHOULD HAVE BEEN RED. THE DEVICE WAS IN USE ON PATIENT AT TIME OF EVENT, THERE WAS NO ADVERSE EVENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19509808 ↗
• DeathApr 15, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE CUSTOMER REPORTED A SENTINEL EVENT WITH THE SYSTEM RESULTING IN A PATIENT EXPIRING WHILE ON THE MONITOR. THE DEVICE WAS IN USE ON PATIENT AT TIME OF EVENT, THERE WAS AN ADVERSE EVENT REPORTED.

  Patient problems: Cardiac Arrest; No Clinical Signs, Symptoms or Conditions

  MAUDE report 19105122 ↗
• MalfunctionDec 29, 2023No Audible Prompt/Feedback; No Audible Prompt/Feedback

  THE CUSTOMER REPORTED SPEAKER MALFUNCTION INOP. THE DEVICE WAS IN USE AT TIME OF EVENT, THERE WAS NO ADVERSE EVENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18418422 ↗
• MalfunctionDec 18, 2023No Audible Prompt/Feedback; No Audible Prompt/Feedback

  IT WAS REPORTED THE DEVICE INDICATES A SPEAKER MALFUNCTION ERROR. IT IS UNKNOWN IF THERE WAS SOUND BEING EMITTED FROM THE DEVICE. THE DEVICE WAS IN CLINICAL USE AT THE TIME OF THE EVENT, NO ADVERSE EVENT OR PATIENT HARM WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18345252 ↗
• MalfunctionDec 4, 2023No Audible Alarm; No Audible Alarm

  CUSTOMER REPORTED THE DESAT ALARMS DID NOT SOUND. PATIENT INVOLVEMENT IS UNKNOWN. THERE WAS NO REPORT OF PATIENT OR USER HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18255902 ↗
• MalfunctionNov 30, 2023No Audible Alarm; No Audible Prompt/Feedback; No Audible Alarm; No Audible Prompt/Feedback

  THE CUSTOMER REPORTED A SPEAKER MALFUNCTION ON THE INTELLIVUE MX700 PATIENT MONITOR. IT IS UNKNOWN IF SOUND WAS STILL COMING FROM THE DEVICE. THE DEVICE WAS NOT IN USE MONITORING A PATIENT AT THE TIME OF THE REPORTED ISSUE. NO ADVERSE PATIENT OR USER EVENT WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18235789 ↗
• MalfunctionNov 21, 2023Device Alarm System; Device Alarm System

  THE CUSTOMER REPORTED THAT THE INVASIVE BLOOD PRESSURE (IBP) ALARMS RESET THEMSELVES TO "OFF" ON THE INTELLIVUE MX700 PATIENT MONITOR DESPITE BEING ENABLED IN THE SETTINGS. IT IS UNKNOWN IF THE DEVICE WAS IN USE MONITORING A PATIENT AT THE TIME OF THE REPORTED ISSUE. NO ADVERSE PATIENT EVENT WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18180661 ↗
• MalfunctionOct 24, 2023Defective Alarm; Defective Alarm

  THE CUSTOMER REPORTED THE PATIENT¿S HEART RATE EXCEEDED THE HIGH LIMIT, BUT NO ALARM GENERATED ON THE PHILIPS PATIENT INFORMATION CENTER IX (PIC IX) COMPUTERS IN NEONATAL INTENSIVE CARE UNIT (NICU) DEPARTMENT. THE DEVICE WAS IN CLINICAL USE AT THE TIME THE ISSUE WAS DISCOVERED. THERE WAS NO ADVERSE EVENT OR PATIENT HARM REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17994778 ↗